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Manufacturing Engineer III

Work mode:  Onsite
Onsite Location(s): 

Zona Franca La Lima, Cartago, CR

Additional Locations:  N/A

Diversity - Innovation - Caring - Global Collaboration - Winning Spirit - High Performance

At Boston Scientific, we’ll give you the opportunity to harness all that’s within you by working in teams of diverse and high-performing employees, tackling some of the most important health industry challenges. With access to the latest tools, information and training, we’ll help you in advancing your skills and career. Here, you’ll be supported in progressing – whatever your ambitions.

About the Role:

 

Evaluates, selects, and applies standard engineering techniques, procedures, and criteria, using judgment in making minor adaptations and modifications. Assignments have clear and specified objectives and require the investigation of a limited number of variables. Improve existing manufacturing processes and act as liaison between production and engineering group in resolving problems encountered on the production floor. Assist with the introduction of new products into the Operations production area.

 

Your Responsibilities Include:

 

· May execute the following responsibilities:

· Be a known leader of effective engineering continuous improvement. The person is recognized for implement systemic solutions, sustainable through time, that minimize human dependances.

· The person is a mentor of younger engineers and contributes to the technical/engineering growth of the area. Supports the existence of strong validations that captures process vulnerabilities and ensure start up after validations are smooth. Supports the development of the technical pipeline for the site.

· Participates and/or leads project teams typically including one of the following: identifying and implementing process/product improvement alternatives to increase/optimize yield, efficiency, throughput, and/or performance; designing, performing, and documenting engineering test experiments to evaluate product/product performance; participating in Quality improvement activities; designing, developing, testing, and validating equipment, tools and fixtures; analyzing and interpreting process models and recommending process improvements; evaluates external process technologies; and other activities of limited scope requiring knowledge of principles and techniques commonly employed in the specific narrow area of assignments.

· Team up with Equipment Engineering to ensure that the implementation of new equipment is constructively aligned with the process needs.

· Participate in equipment and process validation. Write protocols and reports for Equipment Installation Qualification, Operational Qualification and Process Performance Qualification.

· Has working knowledge of Risk Management & Failure mode and effect analysis (FMEA) requirements.

· Interfaces with assemblers, production supervisors, and engineers in troubleshooting problems on the production floor. Arrange and present data in a clear manner so it becomes clear who is the owner and what’s the right direction.

· Coordinates with the appropriate suppliers and other external resources needed in developing and implementing process/product improvement plans.

· Acts independently to implement and follow through. Requires minimum follow up of a supervisor

· Perform root cause analysis of failed product. Excels at Problem Solving/Process improvement tools and methodology, and mentor others/

· Participates in project planning and scheduling.

· Optimize processes for yield improvements, cycle time improvements, and scrap reduction.

· Attends and contributes to product core team meetings. Communicates adequately, has courage, challenge the status quo without compromising relationships. Influences below, flat and above

· Performs responsibilities required by the Quality System and other duties as assigned or requested.

 

What We’re Looking For:

 

· Bachelor’s degree in mechanical, Electromechanical, Electronic, Biomedical, Chemistry, Industrial, Electrical, Industrial Maintenance or Equivalent experience.

· English Level desired: 80-89%.

· Desired knowledge: Process Manufacturing Certification, Problem Solving, Regulatory industry management, Regulatory Affair, Networking, Process Validations, Stadistical and Experimental Analysis, DOE, Solid Works, Transfer Process, MiniTab, Hands & Statisctics, Validation Process, Tools (Statistics, Technical Manuals, Kaizen, Six Sigma), Regulatory industry management.

· At least 3 years of experience in similar position.

· Or an equivalent combination of education and experience.

#CRTA

#CTGTA

 

 

Requisition ID: 621158

 

As a leader in medical science for more than 40 years, we are committed to solving the challenges that matter most – united by a deep caring for human life. Our mission to advance science for life is about transforming lives through innovative medical solutions that improve patient lives, create value for our customers, and support our employees and the communities in which we operate. Now more than ever, we have a responsibility to apply those values to everything we do – as a global business and as a global corporate citizen.

 

So, choosing a career with Boston Scientific (NYSE: BSX) isn’t just business, it’s personal. And if you’re a natural problem-solver with the imagination, determination, and spirit to make a meaningful difference to people worldwide, we encourage you to apply and look forward to connecting with you!


Job Segment: Biomedical Engineering, Six Sigma, Manufacturing Engineer, Industrial, Engineering, Management, Manufacturing

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